Stacey Scirocco
About Stacey Scirocco
Stacey Scirocco serves as a Senior Regulatory Analyst in the Human Research Protection Program (IRB) at Yale University, where she has worked since 2015. With extensive experience at Yale, she has held various roles, including positions in the Yale Cancer Center and the Yale Center for Clinical Investigation.
Work at Yale University
Stacey Scirocco has held multiple positions at Yale University, contributing to various departments over the years. She has been serving as a Senior Regulatory Analyst in the Human Research Protection Program (IRB) since 2019. Prior to this role, she worked as a Regulatory Analyst in the same program starting in 2015. Her experience at Yale also includes a position as Associate Director for Scientific Committees at the Yale Center for Clinical Investigation from 2012 to 2013. Additionally, she was involved with the Yale Cancer Center in an administrative capacity from 1999 to 2007.
Education and Expertise
While specific details about Stacey Scirocco's educational background are not provided, her extensive experience in regulatory analysis and human research protection indicates a strong foundation in these areas. Her roles at Yale University suggest expertise in managing compliance and regulatory issues related to human subjects in research, particularly within the context of clinical investigations.
Background
Stacey Scirocco's professional journey at Yale University spans over two decades, beginning in 1999. Her career has evolved through various roles, primarily focusing on regulatory analysis and administration within the healthcare and research sectors. Her long-term commitment to Yale University reflects her dedication to advancing research protection and compliance in human subjects research.
Achievements
Stacey Scirocco has made significant contributions to the Human Research Protection Program at Yale University through her roles as both a Regulatory Analyst and Senior Regulatory Analyst. Her experience in the Yale Cancer Center and the Yale Center for Clinical Investigation has equipped her with a comprehensive understanding of the regulatory landscape governing human research. Her work supports the ethical conduct of research involving human subjects.